BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    ACE SUPRACONDYLAR PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Medi Lift Essential Eye Mask

    FDA 510(k)
    FDA Class 2 ·Neurology

    PENTAX Medical EPK-i7010 Video Processor with GI Family

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    AUTOSOFTÂ XC

    FDA Adverse Event
    Injury ·UNOMEDICAL A/S·Product code FPA·October 1, 2024

    SECURA DR

    FDA Adverse Event
    Death ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·February 8, 2013

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·July 11, 2014

    TELIGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 6, 2011

    1820334-2020-01805

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FOZ·October 5, 2020